FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TANGENT II
K Number: K883974
·
Decision Oct 20, 1988
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
28
Applicant Total
69
Review Days
30
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Basic Information
- Device Name
- TANGENT II
- K Number
- K883974
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1980
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Fischer Imaging Corp.
- Date Received
- September 20, 1988
- Decision Date
- October 20, 1988
- Product Code
- IZZ
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| IZZ | Table, Radiographic, Non-Tilting, Powered | FDA class 2 | Radiology |
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Other Clearances by Fischer Imaging Corp.
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|---|---|---|---|
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| K973400 | MAMMOTEST ADAPTER DRIVER | Nov 10, 1997 | Substantially Equivalent |
| K964806 | MD-1835 | Mar 4, 1997 | Substantially Equivalent |
| K961207 | EP-X BIPLANE | Aug 20, 1996 | Substantially Equivalent |
| K961022 | TANGENT VI TABLE | May 3, 1996 | Substantially Equivalent |
| K950291 | DIGITAL 625HF | Mar 23, 1995 | Substantially Equivalent |
| K945619 | ATHENA HFX | Mar 23, 1995 | Substantially Equivalent |
| K944147 | MICRO X-50 HF | Sep 16, 1994 | Substantially Equivalent |